Canonical Allele Identifier: PA2826270372
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18094
ClinVar RCV Id: RCV000547582 RCV000826088 RCV002272025 RCV000019721 RCV000084566
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191230.1:p.Ala695Thr
CA090906
NM_001204301.2:c.2083G>A